Human Genetics. Proceedings of the 6th International Congress..., Sept. 13-18, 1981, Jerusalem: Medical aspects. II, Teil 2Batsheva Bonné-Tamir Liss, 1982 - 619 Seiten |
Im Buch
Ergebnisse 1-3 von 82
Seite 67
... affected sibpairs as sharing 2 , 1 , or 0 HLA haplotypes identical by descent . In the case of Gm allotypes , this method was not utilized since it was sometimes difficult to distinguish 2 and 1 haplotype sharing between affected ...
... affected sibpairs as sharing 2 , 1 , or 0 HLA haplotypes identical by descent . In the case of Gm allotypes , this method was not utilized since it was sometimes difficult to distinguish 2 and 1 haplotype sharing between affected ...
Seite 69
... Affected Unaffected Affected Unaffected Affected Unaffected 16 14 13 8 3 6 0 13 0 11 0 2 < 6.0 x 10 NS One affected sibling used to determine disease - associated haplotypes in each family was excluded from this analysis . The P value ...
... Affected Unaffected Affected Unaffected Affected Unaffected 16 14 13 8 3 6 0 13 0 11 0 2 < 6.0 x 10 NS One affected sibling used to determine disease - associated haplotypes in each family was excluded from this analysis . The P value ...
Seite 81
... AFFECTED SIBPAIR METHOD The theory of the affected sibpair method has been investigated by a number of workers , who have made many different assumptions about the penetrance parameters for the genotypes at the “ disease " locus , and ...
... AFFECTED SIBPAIR METHOD The theory of the affected sibpair method has been investigated by a number of workers , who have made many different assumptions about the penetrance parameters for the genotypes at the “ disease " locus , and ...
Inhalt
Carrier Detection | 15 |
HLA and Infectious Diseases | 37 |
HLA and Diabetes | 55 |
Urheberrecht | |
49 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
abnormalities activity addition affected allele analysis antigens appears association binding biochemical blood carrier cells changes chromosome clinical common complex cultured defect deficiency Department determined diabetes diabetes mellitus diagnosis disease disorders distribution dominant environmental enzyme estimated et al evidence expression factors fibroblasts findings frequency gene glucose haplotypes heterogeneity heterozygotes Hum Genet human hypertension IDDM immune important increased indicated individuals inheritance internalization involved Italy levels linkage linked locus lysosomal major marker measured Medical method mode of inheritance multiple mutant neural tube normal observed occur origin pairs parents patients phenotype population possible pregnancy prenatal present problems protein recently receptor recessive relative reported Research response risk screening showed shown significant specific structure studies suggested syndrome Table tissue trait translocation tumor twin ulcer University values York